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  • USP27X variants underlying X-linked intellectual disability disrupt protein function via distinct mechanisms

    USP27X variants underlying X-linked intellectual disability disrupt protein function via distinct mechanisms
    Authors:Intisar Koch, Sanford ResearchMaya Slovik, Hebrew University of JerusalemYuling Zhang, Shandong UniversityBingyu Liu, Shandong UniversityMartin Rennie, University of GlasgowEmily Konz, Sanford ResearchBenjamin Cogne, Nantes UniversitéMuhannad Daana, Clalit Health Care ServicesLaura Davids, Children’s Healthcare of AtlantaIllja J. Diets, Radboud UniversityNina B. Gold, Massachusetts General Hospital for ChildrenAlexander M. Holtz, Harvard Medical SchoolBertrand Isidor, Nantes UniversitéHagar Mor-Shaked, Hebrew University of JerusalemJuanita Neira Fresneda, Emory UniversityKaren Y. Niederhoffer, University of AlbertaMathilde Nizon, Nantes UniversitéRolph Pfundt, Radboud UniversityM.E.H. Simon, University Medical Center UtrechtA.P.A. Stegmann, Maastricht UniversityMaria J. Guillen Sacoto, GeneDxMarijke Wevers, Radboud UniversityTahsin Stefan Barakat, Erasmus MC UniversityShira Yanovsky-Dagan, Hadassah Medical CenterBoyko S. Atanassov, Roswell Park Comprehensive Cancer CenterRachel Toth, University of DundeeChengjiang Gao, Shandong UniversityFrancisco Bustos, Sanford ResearchTamar Harel, Hebrew University of Jerusalem
    Date:2024
    Publisher:EMBO Press
    Publication Version:Final Published Version
    License:Creative Commons Attribution 4.0 International